Source: GWASDB

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs10759944
rs10759944
0.925 0.080 9 97794690 intron variant A/G snv 0.72
CUI: C0020676
Disease: Hypothyroidism
Hypothyroidism
0.710 1.000 2 2011 2014
dbSNP: rs10759944
rs10759944
0.925 0.080 9 97794690 intron variant A/G snv 0.72
CUI: C0549473
Disease: Thyroid carcinoma
Thyroid carcinoma
0.700 1.000 3 2009 2013
dbSNP: rs10759944
rs10759944
0.925 0.080 9 97794690 intron variant A/G snv 0.72
CUI: C0162701
Disease: Polysomnography
Polysomnography
0.700 1.000 1 2012 2012